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[利用固定化金属离子亲和色谱法纯化抗-HBcAg单克隆抗体]

[Purification of anti-HBcAg monoclonal antibodies using immobilized metal ion affinity chromatography].

作者信息

Zhu Ji, Yi Yu, Wu Yinfei, Zhu Keyin, Mei Jianfeng, Chen Jianshu, Ying Guoqing

机构信息

College of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou 310014, China.

出版信息

Sheng Wu Gong Cheng Xue Bao. 2009 Oct;25(10):1572-8.

Abstract

Anti-HBcAg monoclonal antibodies from mouse ascites were purified by using immobilized metal ion affinity chromatography. We optimized the conditions of sample loading and elution. The results showed that when the pH stepwise elution was used, the best solution for sample loading was 20 mmol/L phosphate buffer containing 0.5 mol/L sodium chloride at pH 8.0 and the mAb was eluted at pH 5.0. The purity of obtained mAb was more than 85% and recovery reached 80%. When the adsorbed proteins were eluted by using gradient elution of an imidazole, the best solution for loading condition was 20 mmolL phosphate buffer containing 5 mmol/L imidazole at pH 8.0. The purity and recovery of antibody were up to 95%.

摘要

利用固定化金属离子亲和色谱法纯化来自小鼠腹水的抗-HBcAg单克隆抗体。我们优化了上样和洗脱条件。结果表明,采用pH梯度洗脱时,最佳上样溶液为pH 8.0的含0.5 mol/L氯化钠的20 mmol/L磷酸盐缓冲液,单克隆抗体在pH 5.0时洗脱。获得的单克隆抗体纯度大于85%,回收率达到80%。当使用咪唑梯度洗脱吸附的蛋白质时,最佳上样条件溶液为pH 8.0的含5 mmol/L咪唑的20 mmol/L磷酸盐缓冲液。抗体的纯度和回收率高达95%。

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